Mice Lacking a Myc Enhancer That Includes Human SNP rs6983267 Are Resistant to Intestinal Tumors

被引:169
作者
Sur, Inderpreet Kaur [1 ,2 ]
Hallikas, Outi [3 ]
Vaharautio, Anna [1 ,3 ]
Yan, Jian [1 ]
Turunen, Mikko [3 ]
Enge, Martin [1 ]
Taipale, Minna [1 ,3 ]
Karhu, Auli [4 ]
Aaltonen, Lauri A. [4 ]
Taipale, Jussi [1 ,3 ]
机构
[1] Karolinska Inst, Sci Life Ctr, Dept Biosci & Nutr, Stockholm, Sweden
[2] Karolinska Univ Hosp, Clin Res Ctr, Stockholm, Sweden
[3] Univ Helsinki, Biomedicum, Inst Biomed, Genome Scale Biol Program, FI-00014 Helsinki, Finland
[4] Univ Helsinki, Biomedicum, Dept Med Genet, Genome Scale Biol Program, FI-00014 Helsinki, Finland
基金
欧洲研究理事会; 芬兰科学院;
关键词
LONG-RANGE INTERACTION; C-MYC; PROSTATE-CANCER; 8Q24; PROSTATE; BETA-CATENIN; COLON-CANCER; VARIANT; TARGET; SUSCEPTIBILITY; INHIBITION;
D O I
10.1126/science.1228606
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple cancer-associated single-nucleotide polymorphisms (SNPs) have been mapped to conserved sequences within a 500-kilobase region upstream of the MYC oncogene on human chromosome 8q24. These SNPs may affect cancer development through altered regulation of MYC expression, but this hypothesis has been difficult to confirm. We generated mice deficient in Myc-335, a putative MYC regulatory element that contains rs6983267, a SNP accounting for more human cancer-related morbidity than any other genetic variant or mutation. In Myc-335 null mice, Myc transcripts were expressed in the intestinal crypts in a pattern similar to that in wild-type mice but at modestly reduced levels. The mutant mice displayed no overt phenotype but were markedly resistant to intestinal tumorigenesis induced by the APCmin mutation. These results establish that a cancer-associated SNP identified in human genome-wide association studies has a functional effect in vivo.
引用
收藏
页码:1360 / 1363
页数:4
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